Jost Chemical Co
FDA Regulatory Profile
Jost Chemical Co has 3 FDA recalls, 8 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest recall
- F-1297-2023 · Class II · Jun 22, 2023
- Latest inspection
- Aug 14, 2025 · VAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 3 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 8 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| F-1297-2023 | Class II | Zinc Sulfate Monohydrate, USP, Powder. Net Wt: 55 lb / 25 kg. Jost Chemical 8150 Lackland, St… | Jun 22, 2023 |
| F-0968-2023 | Class III | Jost Chemical Magnesium Citrate Tribasic Hydrate, USP, Powder, Net Wt 110 lb/ 50 kg packaged in bulk… | May 5, 2023 |
| F-0756-2023 | Class III | Magnesium Citrate Tribasic Hydrate, USP, Ultrafine Powder sold in bulk 55 lb fiber box. | Mar 17, 2023 |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Aug 14, 2025 | Saint Louis, MO | Drugs | Voluntary Action Indicated (VAI) | 3001239108 |
| Oct 13, 2023 | Saint Louis, MO | Drugs | Voluntary Action Indicated (VAI) | 3001239108 |
| Aug 25, 2023 | Saint Louis, MO | Drugs | No Action Indicated (NAI) | 3001239108 |
| Jan 21, 2022 | Saint Louis, MO | Drugs | Official Action Indicated (OAI) | 3001239108 |
| Jan 18, 2018 | Saint Louis, MO | Food/Cosmetics | No Action Indicated (NAI) | 3001239108 |
| Aug 24, 2015 | Saint Louis, MO | Drugs | No Action Indicated (NAI) | 3001239108 |
| May 3, 2012 | Saint Louis, MO | Drugs | No Action Indicated (NAI) | 3001239108 |
| Sep 17, 2010 | Saint Louis, MO | Drugs | No Action Indicated (NAI) | 3001239108 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3001239108 | Saint Louis, MO | 8 | Aug 14, 2025 |